Expired nitric oxide after bronchoprovocation and repeated spirometry in patients with asthma

被引:108
作者
Deykin, A
Halpern, O
Massaro, AF
Drazen, JM
Israel, E
机构
[1] Brigham & Womens Hosp, Dept Med, Div Pulm & Crit Care, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
关键词
D O I
10.1164/ajrccm.157.3.9707114
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Compared with normal individuals, subjects with asthma have elevated levels of expired nitric oxide (NO). These levels are hypothesized to reflect the degree of airway inflammation. Expired NO levels rise during the late phase of allergen challenge and decrease in asthmatics after steroid treatment. Isocapnic cold air hyperventilation (ISH) is believed to cause airway narrowing through noninflammatory mechanisms. We measured mixed expired NO in 10 individuals with atopic asthma who underwent both ISH challenge and allergen challenge, and compared these measurements with the change in expired NO that occurred after serial spirometry alone. We found that ambient NO levels affected mixed expired NO. Controlling for inspired NO, we found that repeated spirometry alone produced a significant fall in mixed expired NO (p < 0.01) that was maximal after 30 min (36.6 +/- 8.5% fall). After allergen and ISH challenges, expired NO was elevated relative to levels after repeated spirometry (p < 0.01 and p = 0.065, respectively). In addition, we found that prechallenge expired NO levels were significantly correlated with the magnitude of the late fall in FEV, following allergen challenge (r = 0.80, p < 0.01). These data demonstrate that repeated spirometry results in reduced mixed expired NO and suggest that both ISH and allergen-induced bronchoconstriction share pathobiologic mechanisms that produce increases in mixed expired NO.
引用
收藏
页码:769 / 775
页数:7
相关论文
共 34 条
  • [1] NITRIC-OXIDE MEDIATES CIGARETTE SMOKE-INDUCED VASODILATORY RESPONSES IN THE LUNG
    ALVING, K
    FORNHEM, C
    WEITZBERG, E
    LUNDBERG, JM
    [J]. ACTA PHYSIOLOGICA SCANDINAVICA, 1992, 146 (03): : 407 - 408
  • [2] ALVING K, 1993, EUR RESPIR J, V6, P1368
  • [3] NITRIC-OXIDE - MEDIATOR, MURDERER, AND MEDICINE
    ANGGARD, E
    [J]. LANCET, 1994, 343 (8907) : 1199 - 1206
  • [4] CONSTITUTIVE AND INDUCIBLE NITRIC-OXIDE SYNTHASE GENE-EXPRESSION, REGULATION, AND ACTIVITY IN HUMAN LUNG EPITHELIAL-CELLS
    ASANO, K
    CHEE, CBE
    GASTON, B
    LILLY, CM
    GERARD, C
    DRAZEN, JM
    STAMLER, JS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) : 10089 - 10093
  • [5] BELVISI MG, 1995, ARCH INT PHARMACOD T, V329, P97
  • [6] NITRIC-OXIDE IS THE ENDOGENOUS NEUROTRANSMITTER OF BRONCHODILATOR NERVES IN HUMANS
    BELVISI, MG
    STRETTON, CD
    YACOUB, M
    BARNES, PJ
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 210 (02) : 221 - 222
  • [7] MEASUREMENT OF EXHALED NITRIC-OXIDE IN MAN
    BORLAND, C
    COX, Y
    HIGENBOTTAM, T
    [J]. THORAX, 1993, 48 (11) : 1160 - 1162
  • [8] Busse W W, 1991, Clin Exp Allergy, V21 Suppl 1, P68, DOI 10.1111/j.1365-2222.1991.tb01708.x
  • [9] Contribution of type I NOS to expired gas NO and bronchial responsiveness in mice
    DeSanctis, GT
    Mehta, S
    Kobzik, L
    Yandava, C
    Jiao, AP
    Huang, PL
    Drazen, JM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 273 (04) : L883 - L888
  • [10] GLUCOCORTICOIDS INHIBIT THE INDUCTION OF NITRIC-OXIDE SYNTHASE IN MACROPHAGES
    DIROSA, M
    RADOMSKI, M
    CARNUCCIO, R
    MONCADA, S
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 172 (03) : 1246 - 1252